{"data":{"id":"us-md/md.-code-health-occupations-12-6c-03.2","jurisdiction":"us-md","citation":"Md. Code, Health Occupations § 12–6C–03.2","heading":"","body":"(a) Notwithstanding any other provision of this subtitle, a wholesale distributor applicant or permit holder that prepares sterile drug products shall submit to the Board a report of an inspection conducted by the U.S. Food and Drug Administration or a Board designee:\n(1) At the time of application; and\n(2) On renewal.\n(b) The inspection report required under subsection (a) of this section shall:\n(1) Be conducted within 1 year before the date of application or renewal; and\n(2) Demonstrate compliance with applicable federal good manufacturing practice standards.\n(c) An applicant or permit holder is responsible for obtaining an inspection to meet the requirements of this section.","path":["Article - Health Occupations"],"source_url":"https://mgaleg.maryland.gov/mgawebsite/Laws/StatuteText?article=gho\u0026section=12-6C-03.2","current_through":"2026-01-01","vintage":"","retrieved_at":"2026-09-14T19:58:58Z","sha256":"f960778133d70a29ded61ec1a541250a8320b696f62fcebd73f4628ff1b4b939","source_id":"us-md","stale":false,"prev":"us-md/md.-code-health-occupations-12-6c-03.1","next":"us-md/md.-code-health-occupations-12-6c-04"},"notice":"GroundRules: Original legal text. Not legal advice."}